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Raydent C&B RCB01P

by Ray Co., Ltd

Raydent C&B RCB01P is a Class I device made by Ray Co., Ltd, listed in FDA GUDID since 3 Nov 2022 (UDI-DI 18800003006004), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number18800003006004 UDI-DI Date3 Nov 2022ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Raydent C&B
Generic name
Dental appliance fabrication material, ceramic
Model / reference
RCB01P
Primary DI / UDI-DI
18800003006004
FDA product code
ELJ
GMDN term
Dental appliance fabrication material, ceramic
Device class
Class I
Regulation number
872.3900
GUDID distribution status
Not in Commercial Distribution

Other devices from Ray Co., Ltd

See all devices from Ray Co., Ltd →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)